PillCam-SPECTRA Bleeding-Region Detection (PWDR) L1-512
Unclaimed Principle — open for contribution
This Principle is declared in the catalog but has no reference solver, no pinned dataset, and is not registered on-chain. There is no reward pool. Submitting a cert against this Principle today will record the cert for reproducibility but pay zero PWM.
To claim it as a Bounty #7 contribution: open a PR adding (1) a reference solver, (2) ≥1 dataset pinned to IPFS, (3) updates to the L3 manifest with dataset CIDs. After verifier-agent triple-review, the founders' 3-of-5 multisig signs PWMRegistry.register() and the Principle becomes mineable.
Forward model E
PillCam-SPECTRA Bleeding-Region Detection (PWDR): the v2 physical_with_discrete_readout wrapper around L1-511 analytical core. The forward operator is the composition (threshold_function . L1-511_forward): multispectral capsule frames -> recovered chromophore concentrations (c_HbO2, c_Hb, c_water, c_lipid, c_melanin)(r) via L1-511 -> categorical labels {normal, bleeding, polyp, suspected_neoplasia, mucosal_inflammation}(r) via piecewise-constant threshold function on chromophore concentrations and reduced scattering coefficient mu_s'. The threshold is locally Lipschitz-continuous on the underlying physical state with global Lipschitz constant ~0.10 (per the smoothed-softmax formulation in discrete_readout.threshold_function). Recovery is posed as the joint problem: (i) recover continuous physical state via L1-511 (analytical S1-S4); (ii) apply deterministic threshold to produce categorical readout (S1-S4 inherited via Lipschitz continuity). The gate_substitutions field populates only conservation_substitute (softmax simplex closure on categorical readout); kappa_substitute and h_substitute are null because the physics core retains its analytical kappa and h. Difficulty tier delta = 3 inherited from L1-511. Mismatch parameters extend the L1-511 set: threshold_calibration_uncertainty, between-region_smoothing_artifact, motion-induced_label_flicker, capsule_orientation_mucosal_assignment.
L-DAG
Well-posedness W
- Existence:
- true
- Uniqueness:
- conditional
- Stability:
- conditional
- κ:
- 80
Existence and uniqueness inherited from L1-511 analytical core; threshold function is piecewise-constant and Lipschitz-continuous on the underlying chromophore-concentration state, so existence and uniqueness lift from continuous to discrete readout under the standard categorical-readout argument (PWM_GATE_CLASSES_AND_SCALING.md Case A). Stability inherits L1-511's kappa_eff ~ 15 plus a small additive contribution C_threshold * |threshold_calibration_uncertainty| from per-class threshold-value uncertainty. The threshold-continuity_proof in discrete_readout demonstrates that boundaries between class regions form measure-zero hyperplanes in chromophore space, so misclassification probability scales linearly with chromophore-recovery error away from the boundary.
Solvability C
- Solver class:
- linear-operator + convex optimisation [L1-511 chromophore unmixing] + categorical-readout [argmax / smoothed-softmax threshold] | end-to-end deep neural prior [PillCamNet, GINet] with explicit physics-informed analytical-core regularization
- Convergence rate q:
- 2
- Complexity:
- O(H * W * N_wavelengths * N_chromophores) for stage 1 (inherited from L1-511) + O(H * W * N_classes) for stage 2 threshold evaluation; total ~stage-1-dominated